Self-sampling by cervicovaginal lavage could be an attractive method to detect high-risk human papillomavirus (hr-HPV) infections to identify women with a risk of cervical precancer. The objective of our study was to use self-sampling for the first time in a cross-sectional approach to determine HPV prevalence and genotype distribution. We evaluated participants' acceptance and laboratory results from self-obtained samples versus endocervical brush samples obtained by gynecologists. To determine the sensitivity of both sampling methods in presumed high-and low-prevalence settings, two groups of women 20 to 30 years of age with (n ؍ 55) and without (n ؍ 101) a recent suspicious cytological smear were compared. Overall, 76% (95% confidence interval [95% CI], 65 to 88) of women with and 40% (95% CI, 30 to 49) of women without a recent suspicious cytological smear tested HPV positive. The prevalences of high-risk HPV strains were 71% (95% CI, 59 to 83) and 32% (95% CI, 22 to 41), respectively, for these two groups. The agreement for hr-HPV between the two sampling methods for women with and without suspicious cytology was 84% ( ؍ 0.65; 95% CI, 0.44 to 0.86) and 91% ( ؍ 0.78; 95% CI, 0.64 to 0.92), respectively. Participants rated the user-friendliness of the self-sampling method on a visual analog scale from 0 (easy) to 100 (difficult) with a median of 12. In conclusion, self-sampling by cervicovaginal lavage is a reliable method to determine hr-HPV prevalence and is well accepted by young adult females.Cervical cancer is the second most common cancer in women worldwide, with globally approximately 500,000 new cases and 250,000 deaths each year (http://www.who.int /reproductivehealth/topics/cancers/en/). The strong correlation between cervical cancer and a preceding persistent infection of the cervix with human papillomavirus (HPV) is beyond dispute (2, 18). More than 130 genotypes of HPV have been classified (6), of which about 40 genotypes can infect the anogenital tract (14). Of these 40 genotypes, nearly 20 are thought to be carcinogenic and are classified as high-risk HPV (hr-HPV). Genotypes 16 and 18 alone are associated with approximately 50% of high-grade cervical intraepithelial neoplasia (CIN) and 70% of cervical cancers (4, 20). Anogenital HPV infections are predominantly sexually transmitted, and nearly all sexually active women will be infected at some point during their lifetime (1). Most HPV infections are transient, but persistent infections can progress over years to high-grade CIN or cervical cancer.Vaccines against HPV genotypes 16 and 18 have been available since 2006. Results from clinical trials indicate high effectiveness against high-grade CIN when HPV-naïve girls and women are vaccinated (7,16,17). Numerous industrial countries have implemented vaccination programs to protect girls against infections with HPV types 16 and 18. Target groups for the vaccination are mainly adolescent women preceding their sexual debut. To monitor the impact of the vaccine and the implemented vaccination...